1,4-Fluorochlorobenzene
Linshang Chemical
HS Code |
655158 |
Chemical Formula | C6H3ClF2 |
Molar Mass | 148.54 g/mol |
Appearance | Colorless to pale - yellow liquid |
Boiling Point | 115 - 117 °C |
Melting Point | -39 °C |
Density | 1.307 g/mL at 25 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 3.9 kPa at 25 °C |
Flash Point | 15 °C |
Odor | Characteristic aromatic odor |
As an accredited 1,4-Fluorochlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
Packing | 1,4 - Fluorochlorobenzene in 5 - liter sealed cans for chemical storage. |
Storage | 1,4 - Fluorochlorobenzene should be stored in a cool, well - ventilated area away from heat, sparks, and open flames as it is flammable. Keep it in tightly sealed containers to prevent vapor release. Store it separately from oxidizing agents and incompatible substances. Ensure the storage location has proper spill - containment measures to handle any potential leaks safely. |
Shipping | 1,4 - Fluorochlorobenzene is shipped in tightly - sealed, corrosion - resistant containers. It's transported under regulated conditions, following strict safety protocols due to its chemical nature, ensuring secure delivery. |
Competitive 1,4-Fluorochlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
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As a leading 1,4-Fluorochlorobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
1,4-fluorochlorobenzene is a key raw material in the field of organic synthesis. Due to its special chemical structure, it can participate in a variety of organic reactions and lay the foundation for the construction of complex organic compounds. For example, in the process of drug synthesis, it is often used as a starting material, which can be converted into compounds with specific pharmacological activities through a series of delicate reaction steps. In the preparation of many antibacterial and anti-inflammatory drugs, 1,4-fluorochlorobenzene plays a crucial role in helping pharmaceutical chemists build the required molecular framework.
Furthermore, in the field of pesticide synthesis, 1,4-fluorochlorobenzene also shows extraordinary value. Through ingenious chemical reactions, it can be converted into various high-efficiency pesticide ingredients. Such pesticides have excellent control effects on crop pests, which can protect crops from thriving and ensure agricultural harvests. Due to its stable chemical properties and suitable activity, it can effectively kill pests while having a controllable impact on the environment, meeting the strict requirements of modern green agriculture for pesticides.
In addition, in the field of materials science, 1,4-fluorochlorobenzene also plays a role. It can be used as a key monomer in the synthesis of special functional materials. Polymer materials with unique properties can be prepared through polymerization and other reactions. These materials may have excellent heat resistance, chemical corrosion resistance, or special optical and electrical properties, and are widely used in high-end fields such as electronics and aerospace, contributing to technological innovation and development in related industries.
1,4 - fluorochlorobenzene is a colorless to pale yellow liquid with a unique odor. Its relative density is about 1.25 (water = 1), which makes it heavier than water and will sink to the bottom if mixed with water. The boiling point is between 117 - 119 ° C. At this temperature, 1,4 - fluorochlorobenzene changes from liquid to gaseous. The melting point is about -35 ° C. Below this temperature, it will solidify into a solid state.
1,4-Fluorochlorobenzene is slightly soluble in water. This property is due to the large difference between its molecular structure and that of water, and the weak force between the two, so it is difficult to dissolve each other. However, it can be miscible with most organic solvents, such as ethanol, ether, etc., because the force between it and the organic solvent molecules is sufficient to make it evenly dispersed, so as to achieve miscibility.
The vapor pressure of 1,4-Fluorochlorobenzene has a specific value at a certain temperature, and the vapor pressure reflects the difficulty of volatilization. At room temperature, it has a certain volatility and will evaporate steam. Its vapor density is about 4.6 relative to air, which is heavier than air, so the steam will spread close to the ground. This requires special attention to the diffusion and accumulation of steam in places involving 1,4-fluorochlorobenzene, because it may accumulate in low-lying areas, posing latent risks.
In addition, 1,4-fluorochlorobenzene has a certain refractive index. When light passes through it, refraction will occur. Refractive index is an important manifestation of its optical properties and can be used for analysis work such as purity detection. These physical properties are crucial for understanding the behavioral characteristics of 1,4-fluorochlorobenzene, its state in different environments, and its application in chemical production, analysis and testing.
In terms of reactivity, its electrophilic substitution reaction is slightly slower than that of benzene. The electron-withdrawing effect of fluorine and chlorine reduces the electron cloud density of the benzene ring, which is not conducive to the attack of electrophilic reagents. However, the stability of the aromatic ring makes it possible for such reactions to occur under specific conditions. If under appropriate catalyst and reaction conditions, halogenation, nitration, sulfonation and other electrophilic substitution reactions can occur.
Under normal environmental conditions, 1,4-fluorochlorobenzene is not easy to decompose spontaneously or undergo other violent chemical reactions. Its chemical corrosion resistance is also good. Under normal temperature and pressure, it rarely reacts significantly with many common acids and bases, oxidizing agents, reducing agents and other substances without specific reaction conditions.
However, it should be noted that although its chemical properties are stable, it can also participate in a variety of chemical reactions under extreme conditions of high temperature, high pressure, or special catalysts, showing the changeable characteristics of organic compounds. In short, 1,4-fluorochlorobenzene is chemically stable under general conditions, but under specific environmental and conditions, its chemical activity can also be excited and various transformations occur.
First, p-chloroaniline is used as raw material. First, p-chloroaniline is mixed with hydrofluoric acid and sodium nitrite for diazotization reaction. This process needs to be carefully operated, and the reaction temperature and material ratio should be controlled to convert p-chloroaniline into diazonium salt. Subsequently, the diazonium salt is decomposed under appropriate conditions, and nitrogen gas is released to generate 1,4-fluorochlorobenzene. In this path, the diazotization reaction conditions are critical. If the temperature is too high, it is easy to cause the decomposition of diazonium salt to go out of control, which affects the yield and product purity.
Second, p-dichlorobenzene is used as raw material. Under the action of a specific catalyst, a halogen exchange reaction Selecting a high-efficiency catalyst is of great significance to the reaction process. The reaction is usually carried out in an organic solvent to ensure that the reactants are fully contacted. This process requires attention to the fact that the reaction system is anhydrous, because water will affect the activity of potassium fluoride and reduce the reaction efficiency.
Third, p-fluoroaniline is used as a raw material. Similar to the diazotization reaction process of p-chloroaniline, p-fluoroaniline is diazotized and then interacts with cuprous chloride and other reagents to replace the diazoyl group with chlorine atoms to obtain 1,4-fluorochlorobenzene. In this method, both the diazotization and substitution reaction steps need to precisely control the conditions to ensure the smooth progress of the reaction and
The first words of storage must be in a cool and well-ventilated place. This may be affected by temperature and humidity, high temperature or cause its volatilization to intensify, or cause other chemical reactions. The warehouse should be kept away from fire and heat sources to avoid accidents. And it should be stored separately with oxidants and food chemicals to prevent interaction and danger. The storage place should also have suitable materials to contain leaks. If there is a leak, it can be dealt with in time.
As for transportation, it should not be ignored. Transportation vehicles should ensure that they are in good condition and have corresponding safety facilities. During transportation, they should be protected from exposure to the sun, rain, and high temperature. When handling, they must be lightly loaded and unloaded to prevent damage to packaging and containers and leakage of materials. Transportation personnel should also be familiar with their characteristics and emergency handling methods. In case of emergencies, they can properly deal with them.
In addition, whether it is storage or transportation, they should strictly abide by relevant laws and standards, and make labels so that others can clearly understand their nature and precautions. In this way, 1% 2C4-fluorochlorobenzene is safe and safe during storage and transportation, and will not cause harm to personnel and the environment.
In the synthesis of medicine, it is often an important intermediate. In the creation of medicine, such as the preparation of some antibacterial and anti-inflammatory drugs, 1,4-fluorochlorobenzene can be used as a starting material. After a series of delicate chemical reactions, various chemical groups are added to shape a specific molecular structure, and then a drug component with unique pharmacological activity is formed. This is because of the characteristics of fluorine and chlorine atoms in its structure, which can affect the ability of drugs to bind to biological targets and improve drug efficacy and selectivity.
In the process of pesticide manufacturing, 1,4-fluorochlorobenzene is also indispensable. The research and development of many high-efficiency pesticides is based on it to build a molecular skeleton. Because it can endow pesticides with specific biological activities, such as interfering with the nervous system of pests, or inhibiting the growth mechanism of weeds, it can achieve effective prevention and control of crop diseases, pests and weeds, and ensure agricultural harvests.
Furthermore, in the field of materials science, 1,4-fluorochlorobenzene also has its uses. In the synthesis of special polymer materials, this compound can be introduced to improve the properties of the material. For example, introducing it into the polymer structure can change the thermal stability, mechanical properties and chemical stability of the material. Due to the interaction between fluorine and chlorine atoms and polymer molecular chains, the intermolecular forces can be adjusted to optimize the overall characteristics of materials, making them suitable for high-end fields such as aerospace and electronics that require special properties of materials.
In summary, 1,4-fluorochlorobenzene plays a pivotal role in many key fields such as medicine, pesticides and materials science, and has made great contributions to the development of various fields.
1,4-fluorochlorobenzene is a colorless and transparent liquid with a pungent odor. Its boiling point is about 128 ° C. This property makes 1,4-fluorochlorobenzene change from liquid to gaseous when heated to this temperature, which is conducive to separation and purification by distillation. The melting point is about -34 ° C, indicating that at lower temperatures, 1,4-fluorochlorobenzene will solidify into a solid state.
1,4-fluorochlorobenzene has a higher density than water, about 1.24g/cm ³. When mixed with water, it will sink to the bottom. This property can be used for preliminary separation and identification of liquids with lower density such as water. It is insoluble in water because it is an organic compound, and water is an inorganic substance with strong polarity. According to the principle of similar phase solubility, the polarity difference is large, resulting in the two being insoluble. However, 1,4-fluorochlorobenzene is soluble in organic solvents such as ethanol and ether. Because of its similarity to the intermolecular forces of these organic solvents, it conforms to the law of similar phase solubility. In organic synthesis reactions, its solubility is often used to select an appropriate organic solvent as the reaction medium.
1,4-fluorochlorobenzene has a certain degree of volatility. It will gradually evaporate into the air at room temperature and pressure. When using and storing, it is necessary to pay attention to sealing to prevent its volatilization loss and pollution to the environment. At the same time, because of its pungent odor, it will stimulate people's respiratory tract, eyes, etc. after evaporation. Therefore, the operation should be carried out in a well-ventilated environment and protective measures should be taken.
1,4-fluorochlorobenzene is stable in nature, and it is a colorless liquid at room temperature and pressure, with a special odor. Due to the presence of fluorine and chlorine halogen atoms, its chemical activity is different from that of ordinary benzene derivatives. Fluorine atoms have strong electronegativity, which decreases the electron cloud density of the benzene ring and decreases the activity of electrophilic substitution reactions. Although chlorine atoms also have electron-absorbing induction effects, they are weak. The combined action of the two makes the electrophilic substitution activity of 1,4-fluorochlorobenzene lower than that of benzene. However, under specific conditions and the action of catalysts, such reactions can still occur. For example, when mixed with nitric acid and sulfuric acid, nitro
1,4-fluorochlorobenzene can be substituted with fluorine and chlorine atoms. Under alkaline conditions or specific nucleophiles, halogen atoms can be replaced by other groups, such as hydroxyl substitutions to form corresponding phenolic compounds. This reaction condition needs to be strictly controlled, because different reaction conditions will affect the substitution selectivity and reaction rate.
In addition, 1,4-fluorochlorobenzene is flammable, can burn in case of open flame or hot topic, and can cause violent reactions when in contact with oxidants. When storing and using, pay attention to fire protection, explosion protection, and operate in accordance with relevant safety regulations. Due to its halogen-containing atoms, combustion may produce toxic halogenated hydrogen gas, which is harmful to the environment and human body. When handling waste containing 1,4-fluorochlorobenzene, environmental protection requirements should be followed and appropriate methods should be adopted to avoid polluting the environment.
One is to use p-chloroaniline as the initial raw material. First, it is diazotized with sodium nitrite in the presence of hydrochloric acid to form a diazonium salt. This reaction requires strict control of temperature, usually carried out in a low temperature environment (about 0-5 ° C) to prevent the decomposition of diazonium salts. After generating diazonium salts, it reacts with fluorobenzene to obtain fluorobenzene precipitation. After the precipitation is separated and dried, it is heated and decomposed to obtain 1,4-fluorochlorobenzene. In this process, precise control of the diazotization reaction is crucial, and factors such as temperature and the concentration of the reactants will affect the reaction results.
The second is to use p-chlorophenol as the starting material. Let p-chlorophenol react with fluorinating reagents, such as potassium fluoride, under the presence of suitable solvents and catalysts. The reaction usually needs to be carried out at a higher temperature and appropriate pressure to promote the substitution of fluorine atoms to hydroxyl groups, so as to obtain 1,4-fluorochlorobenzene. The solvent and catalyst selected for the reaction have a great influence on the reaction rate and yield, and it needs to be carefully screened.
The third is to use p-dichlorobenzene as the raw material. Under the action of a specific catalyst, it is selectively fluorinated with the fluorinating agent. The key to this reaction is to find a highly selective catalyst to ensure that the fluorination reaction mainly occurs at the position of one of the chlorine atoms, resulting in the formation of the target product 1,4-fluorochlorobenzene. The activity and selectivity of the catalyst and the optimization of the reaction conditions play a decisive role in the success of the preparation method.
First, it is related to storage. 1,4-fluorochlorobenzene should be placed in a cool and well ventilated place. Because of its certain volatility and flammability, if it is in a high temperature environment, the volatile concentration will increase, and in case of open fire or sparks, there is a risk of fire. And it may be harmful to the environment, so it should be kept away from fire and heat sources to prevent accidents. In addition, the storage area needs to be equipped with appropriate equipment to contain leaks. If a leak occurs, it can be collected in time to prevent it from spreading to the environment and polluting soil, water, etc. It should also be stored separately from oxidants, edible chemicals, etc., and must not be mixed. Because 1,4-fluorochlorobenzene comes into contact with oxidants, or reacts violently, it can cause dangerous conditions.
Second, about transportation. When transporting, make sure that the container does not leak, collapse, fall or damage. Because 1,4-fluorochlorobenzene leaks, it not only pollutes the environment, but also may endanger the health of transporters. Transportation vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. Once a leak or fire occurs on the way, it can be dealt with in time. During transportation, it is necessary to prevent exposure to the sun, rain and high temperature. Summer transportation should pay special attention to the fact that high temperature will enhance the volatilization of 1,4-fluorochlorobenzene and increase the risk factor. At the same time, follow the prescribed route and do not stop in residential areas and densely populated areas. In this way, the potential harm to the public can be reduced. In short, when storing and transporting 1,4-fluorochlorobenzene, it must be operated in strict accordance with relevant regulations, and must not be negligent to ensure the safety of personnel and the environment from pollution.

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